CN106609276A - Recombined nucleic acid fragment RecCR020260 and detection method thereof - Google Patents
Recombined nucleic acid fragment RecCR020260 and detection method thereof Download PDFInfo
- Publication number
- CN106609276A CN106609276A CN201510691321.5A CN201510691321A CN106609276A CN 106609276 A CN106609276 A CN 106609276A CN 201510691321 A CN201510691321 A CN 201510691321A CN 106609276 A CN106609276 A CN 106609276A
- Authority
- CN
- China
- Prior art keywords
- sequence
- primer
- seq
- nucleotide
- specific recognition
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Landscapes
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
Abstract
The invention provides a recombined nucleic acid fragment and a detection method thereof. The invention further provides a breeding method for a rice plant containing the recombined nucleic acid fragment. Foreground selection and background selection are conducted on a recombined plant through molecular markers, and the rice plant containing the recombined nucleic acid fragment is obtained.
Description
Technical field
The application is related to full-length genome selection and use technology.Specifically, the application relates to the use of
Full-length genome selection and use technology selection-breeding contains the rice plant of recombinant nucleic acid fragment, and thus
And the recombinant nucleic acid fragment and its detection method of acquisition.
Background technology
Brown paddy plant hopper, scientific name Nilaparvata lugens (), belong to Homoptera, Delphacidae.It is brown
Plant hopper is monophagy insect, only takes food Oryza sativa L., and with happiness temperature, cold tolerance is weak, growth cycle
It is short, migrate at a distance, the feature such as fulminant and wildness.Brown paddy plant hopper is typical pierce-suck type evil
Worm, is made a living with taking food phloem and xylem sap, and food ingestion is big, breeding is fast, once produce shockingly
Send out, No kernels or seeds are gathered, as in a year of scarcity can to cause damage area.Further, it is also possible to propagate Virus Diseases of Rice (such as:
Grass-like bushy stunt and tingia dwarf wilt), serious harm is also resulted in Rice Production.
It is since the eighties in 20th century, identified more than 30 from wild rice and cultivated rice
Individual brown planthopper resistant site.Due to the complexity of brown paddy plant hopper phenotypic evaluation, cause just to clone in recent years
The Individual genes such as Bph14, Bph26 and Bph3 (Du etc., PNAS.2009,106 (52):
22163-22168;Tamura etc., Sci Rep.2014,4:5872;Liu etc., Nature
Biotechnology.2015,33:301-305).In addition, as brown planthopper resistant kind is in production
In continuous utilization, brown paddy plant hopper gradually strengthens to the adaptability of kind.Some are wide in production
The general resistant variety for utilizing just gradually is losing (Deen etc., the Rice Genet of the resistance to brown paddy plant hopper
Newsl.2010,25:70-72)。
At present, brown paddy plant hopper preventing and treating still relies upon chemical pesticide, not only increases production cost, pollutes ring
Border, and promote brown paddy plant hopper Drug resistance to strengthen.As can be seen here, the cultivation of brown planthopper resistant new varieties
Demand is very urgent.
The content of the invention
On the one hand, this application provides recombinant nucleic acid fragment, which is selected from:I) comprising SEQ ID NO:
The sequence or its fragment of the nucleotide of sequence 485-591 position shown in 1 or its variant or its complementary series;
Ii) comprising SEQ ID NO:The sequence of sequence shown in 1 or its fragment or its variant or its complementary sequence
Row;Iii) comprising SEQ ID NO:The sequence or its piece of the nucleotide of sequence 629-875 position shown in 2
Section or its variant or its complementary series;Iv) comprising SEQ ID NO:The sequence of sequence shown in 2 or
Its fragment or its variant or its complementary series;And the combination of above fragment.In an embodiment
In, the recombinant nucleic acid fragment is genome recombination nucleic acid fragment.
Additionally, this application provides the primer of the detection recombinant nucleic acid fragment, which is selected from:(I) it is special
Opposite sex identification SEQ ID NO:The forward primer of the sequence of the nucleotide of sequence 1-485 position shown in 1 and
Specific recognition SEQ ID NO:The sequence of the nucleotide of sequence 591-1041 position shown in 1 it is reverse
Primer;(II) combination of first group of primer pair and second group of primer pair below, which includes (a) first
Group primer pair:Specific recognition SEQ ID NO:The sequence of the nucleotide of sequence 1-485 positions shown in 1
The forward primer and specific recognition SEQ ID NO of row:The nucleoside of sequence 486-590 positions shown in 1
The reverse primer of the sequence of acid;(b) second group of primer pair:Specific recognition SEQ ID NO:
The forward primer and specific recognition SEQ of the sequence of the nucleotide of sequence 486-590 positions shown in 1
ID NO:The reverse primer of the sequence of the nucleotide of sequence 591-1041 positions shown in 1;(III) it is special
Opposite sex identification is comprising SEQ ID NO:The sequence of the nucleotide of sequence 485-486 positions shown in 1 is just
SEQ ID NO are included to primer and specific recognition:The nucleotide of sequence 590-591 positions shown in 1
Sequence reverse primer;(IV) specific recognition includes SEQ ID NO:Sequence shown in 1
The forward primer and specific recognition SEQ ID NO of the sequence of 485-486 positions nucleotide:Shown in 1
The reverse primer of the sequence of sequence 591-1041 positions nucleotide;(V) specific recognition SEQ ID
NO:The forward primer and specific recognition bag of the sequence of the nucleotide of sequence 1-485 positions shown in 1
The NO of ID containing SEQ:The reverse primer of the sequence of the nucleotide of sequence 590-591 positions shown in 1;With
/ or optionally, (VI) specific recognition SEQ ID NO:The nucleoside of sequence 1-629 positions shown in 2
The forward primer and specific recognition SEQ ID NO of the sequence of acid:Sequence shown in 2
The reverse primer of the sequence of 875-1234 positions nucleotide;(VII) the 3rd group of primer pair and the below
The combination of four groups of primer pairs, which includes (c) the 3rd group of primer pair:Specific recognition SEQ ID NO:
The forward primer and specific recognition SEQ ID of the sequence of the nucleotide of sequence 1-629 positions shown in 2
NO:The reverse primer of the sequence of the nucleotide of sequence 630-874 positions shown in 2;(d) the 4th group
Primer pair:Specific recognition SEQ ID NO:The sequence of the nucleotide of sequence 630-874 positions shown in 2
The forward primer and specific recognition SEQ ID NO of row:The cores of sequence 875-1234 positions shown in 2
The reverse primer of the sequence of thuja acid;(VIII) specific recognition includes SEQ ID NO:Sequence shown in 2
The forward primer and specific recognition for arranging the sequence of 629-630 positions nucleotide includes SEQ ID
NO:The reverse primer of the sequence of the nucleotide of sequence 874-875 positions shown in 2;(IX) specificity
Identification includes SEQ ID NO:The forward direction of the sequence of the nucleotide of sequence 629-630 positions shown in 2 is drawn
Thing and specific recognition SEQ ID NO:The sequence of the nucleotide of sequence 875-1234 positions shown in 2
Reverse primer;(X) specific recognition SEQ ID NO:The nucleoside of sequence 1-629 positions shown in 2
The forward primer and specific recognition of the sequence of acid includes SEQ ID NO:Sequence shown in 2
The reverse primer of the sequence of 874-875 positions nucleotide.
In one embodiment, for expanding SEQ ID NO:The primer pair of sequence shown in 1 is,
For example, 5 '-GGTCCTCTTCCTCCTCGCCTAC-3 ', 5 '-TGCTTTGCCCGTT
GATTGATGT-3’.For detecting SEQ ID NO:The sequencing primer of sequence shown in 1 is, example
Such as, 5 '-GGTCCTCTTCCTCCTCGCCTAC-3 ';With 5 '-TGCTTTGCCCGTT
GATTGATGT-3’。
In another embodiment, for expanding SEQ ID NO:The primer pair of sequence shown in 2
For, for example, 5 '-GGATTGCCTTGGTTGCTTGGTTA-3 ', 5 '-TCTGTCCTTG
TTTCCGTCCCTGT-3’.For detecting SEQ ID NO:The sequencing primer of sequence shown in 2
For, for example, 5 '-GGATTGCCTTGGTTGCTTGGTTA-3 ';With 5 '-TCTGTCC
TTGTTTCCGTCCCTGT-3’。
On the other hand, this application provides selection-breeding contains the side of the rice plant of recombinant nucleic acid fragment
Method, which is included using the Oryza sativa L. recipient plant parent without genes of interest pack section as recurrent parent,
Which is hybridized with the Oryza sativa L. donor plant containing genes of interest pack section, then will be resulting
Cenospecies be returned with recurrent parent, then the step of resulting backcrossing kind is carried out selfing,
Foreground selection and Foreground selection are carried out to plant of recombinating using molecular marker wherein.For example, it is described
Recombinant nucleic acid fragment is as previously mentioned.
In the above-mentioned methods, for the foreground selection molecular marker selected from BphC03ID03,
One or more in RM16165 and RM16211;And/or utilize Oryza sativa L. full-length genome breeding
Chip carries out the Foreground selection.
In one embodiment, the selection-breeding that the application is provided contains brown planthopper resistant gene group recombinant nuclear
The method of the rice plant of acid fragment, which comprises the following steps:1) recurrent parent is planted with donor
Thing is hybridized, then resulting cenospecies and recurrent parent are returned, and obtains backcrossing one
Generation, using favorable selection labelling BphC03ID03 and negative itemsets labelling RM16165,
RM16211 carries out the unilateral homologous recombination fragment screening of brown planthopper resistant gene pack section to which, and
Using Oryza sativa L. full-length genome breeding chip, such as RICE6K carries out Foreground selection to which;2)
Background is selected to reply preferably restructuring individual plant (this generation background recovery value is more than 75%) with samsara parent
This is returned again, obtains second backcross generation, using favorable selection labelling BphC03ID03 pair
Which is detected, selects the restructuring individual plant containing brown planthopper resistant gene pack section, then using water
Rice full-length genome breeding chip, such as RICE6K carry out Foreground selection to which;3) select background
The restructuring individual plant (this generation background recovery value is more than 87.5%) replied is with recurrent parent again
It is returned, is obtained third backcross generation, is selected using favorable selection labelling BphC03ID03 and negative sense
Select labelling RM16165, RM16211 which is carried out brown planthopper resistant gene pack section opposite side it is same
Source recombinant fragment screening, and Oryza sativa L. full-length genome breeding chip is utilized, such as RICE60K is right
Which carries out Foreground selection;And 4) select introgressed segment little, and the restructuring individual plant that background is replied
(background recovery value is more than 93.75%), by the restructuring individual plant selfing chosen once, obtains selfed seed,
Which is detected using favorable selection labelling BphC03ID03, and utilize Oryza sativa L. full-length genome
Breeding chip, such as RICE60K, carry out Foreground selection to which, and final acquisition resists brown containing homozygosis
The Oryza sativa L. of plant hopper genome recombination nucleic acid fragment and background reply (background recovery value is more than 99%) is planted
Strain.
In another embodiment, adopt when carrying out foreground selection to plant of recombinating using molecular marker
Amplimer, including:For the primer pair of amplifier molecule labelling BphC03ID03, its
Middle forward primer is 5 '-GCAAGAATCCGACGCCATAA-3 ', and reverse primer is
5’-CTCTGCTCCTTGCTCTAATCCTCT-3’;For amplifier molecule labelling
The primer pair of RM16165, wherein forward primer are 5 '-GGTTAACCAAGAGGAAA
GGAACC-3 ', reverse primer are 5 '-GCTTTGCAACTCACTGTTGTTACG-3 ';
For the primer pair of amplifier molecule labelling RM16211, wherein forward primer is 5 '-AATGCTA
ATGGCGACTGACTTCG-3 ', reverse primer are 5 '-ATGGGCTTGTTTGATT
GCATCC-3’。
Another aspect, this application provides the method for detection recombinant nucleic acid fragment, which includes basis
Foregoing recombinant nucleic acid fragment design specific primer, is carried out by template of testing gene group
PCR reacts, and the step of analyze pcr amplification product.Specifically, for example, the primer is such as
It is front described.Selectively, pcr amplification product is analyzed using Sanger sequencing.
Specifically, in the method for the detection recombinant nucleic acid fragment that the application is provided, for expanding
And detection SEQ ID NO:The primer combination of sequence shown in 1 is as follows:Amplimer, including forward direction
Primer:5 '-GGTCCTCTTCCTCCTCGCCTAC-3 ', reverse primer:5’-TGCTTTG
CCCGTTGATTGATGT-3’;Sequencing primer, including forward primer:5’-GGTCCTCTT
CCTCCTCGCCTAC-3 ', and reverse primer:5’-TGCTTTGCCCGTTGATT
GATGT-3’.Methods described with testing sample genomic DNA as template, using above-mentioned amplification
Primer enters performing PCR amplification, then the amplified production for obtaining is surveyed using above-mentioned sequencing primer
Sequence, if sequencing result and SEQ ID NO:1 sequence is consistent or complementary, then contain in testing sample
SEQ ID NO:Homologous recombination fragment shown in 1.
In addition, the application provide detection recombinant nucleic acid fragment method in, for amplification and
Detection SEQ ID NO:The primer combination of sequence shown in 2 is as follows:Amplimer, including forward direction draws
Thing:5 '-GGATTGCCTTGGTTGCTTGGTTA-3 ', reverse primer:5’-TCTGT
CCTTGTTTCCGTCCCTGT-3’;Sequencing primer, including forward primer:5’-GGATTG
CCTTGGTTGCTTGGTTA-3 ', and reverse primer:5’-TCTGTCCTTGTTTCC
GTCCCTGT-3’.Methods described with testing sample genomic DNA as template, using above-mentioned
Amplimer enters performing PCR amplification, then the amplified production for obtaining is entered using above-mentioned sequencing primer
Row sequencing, if sequencing result and SEQ ID NO:2 sequences are consistent or complementary, then in testing sample
Containing SEQ ID NO:Homologous recombination fragment shown in 2.
Determined by detection and contain in testing sample SEQ ID NO:1 and/or SEQ ID NO:
The recombinant nucleic acid fragment of sequence shown in 2, you can contain resistant gene in determining testing sample
Recombinant nucleic acid fragment.
Additionally, present invention also provides the test kit of detection recombinant nucleic acid fragment, which is included as front
The primer stated.
Further, present invention also provides screening the rice plant containing recombinant nucleic acid fragment or
The method of seed, whether which contains as previously mentioned in including the genome for detect rice plant to be measured
Recombinant nucleic acid fragment the step of.In one embodiment, using foregoing primer examining
Whether survey in the genome of rice plant to be measured containing foregoing recombinant nucleic acid fragment.Another
In one embodiment, the method using foregoing detection recombinant nucleic acid fragment is to be measured to detect
Whether foregoing recombinant nucleic acid fragment is contained in the genome of rice plant.In another enforcement
In scheme, whether detected using foregoing test kit in the genome of rice plant to be measured
Containing foregoing recombinant nucleic acid fragment.
It yet still another aspect, this application provides containing the application by what methods described screening was obtained
The rice plant or its seed of disclosed recombinant nucleic acid fragment.
What the application was provided contains brown planthopper resistant gene based on full-length genome selection and use technology selection-breeding
Group recombinant nucleic acid fragment rice plant method, with it is quick, accurate, stablize three big features.
Only pass through the transformation of five generations, you can only by target gene group fragment importing acceptor material, and while
Realize the reply of background.The acceptor material of the application improvement is for ' Lu perfume 618B ', is with
Odor type sterile line ' 618A ' the supporting maintainer of Lu perfume of low amylose content.Using above-mentioned
Method, ' in the case of the perfume original advantages of 618B ' of Lu, can improve its brown paddy plant hopper retaining
Resistance.Further, stable containing can be obtained by least first cross, generation backcrossing
Brown Planthopper Resistance fragment ' Lu perfume 618A ', then cenospecies Brown Planthopper Resistance is realized by combo
Increase substantially.Meanwhile, the recombinant nucleic acid fragment that the application is provided is tight with Brown Planthopper Resistance
Correlation, can be applied to the cultivation of other kinds as Resistance resource.
Description of the drawings
Fig. 1 is CR020260 Oryza sativa L. RICE60K full-length genome breedings in the embodiment of the present application 1
Chip detection result;Wherein, square frame indicated by abscissa numeral represents 12 dyeing of Oryza sativa L. successively
Body, vertical coordinate numeral are the physical location [with megabasse (Mb) as unit] on rice genome,
Lycoperdon polymorphum Vitt lines represent receptor parent, and ' Lu perfume 618B ' genotype, black lines represent donor parents
' magnificent 3418B ' genotype, it is consistent i.e. without polymorphic region that white line represents two parent genotypes
Section.The brown planthopper resistant that lines display block is as imported at No. 3 chromosome black round dot in figure
Genome recombination nucleic acid fragment RecCR020260.
Fig. 2 is RecCR020260 upstreams homologous recombination sequencing fragment ratio in the embodiment of the present application 2
To result;Asterisk shown in figure represents identical base in comparison result, and in figure, CR020260 is
The new lines of acquisition, T004 are that ' Lu perfume 618B ', R002 are donor parents ' China to receptor parent
3418B’。
Fig. 3 is RecCR020260 downstreams homologous recombination sequencing fragment ratio in the embodiment of the present application 2
To result.
Fig. 4 is the structure of RecCR020260 both sides homologous recombination fragment in the embodiment of the present application 2
Figure;Wherein, (A) it is upstream homologous recombination fragment structure figure;(B) it is downstream homologous recombination fragment
Structure chart, top base are donor ' SNP the or InDel labellings of magnificent 3418B ', lower section alkali
Base is receptor ' SNP the or InDel labellings of Lu perfume 618B '.Lycoperdon polymorphum Vitt section is from ' Lu
Fragrant 618B ' genomic segments, black section be from ' magnificent 3418B ' genomic segments,
White section is homologous recombination section, and abscissa is fragment length, with base pairs (bp) is
Unit.
Fig. 5 is qualification result in CR020260 Brown Planthopper Resistances room in the embodiment of the present application 3;
Shown in figure, blade is followed successively by:(A) high sense brown paddy plant hopper kind ' coming No. 1 in platform ';(B) original
Plant ' Lu perfume 618B ';(C) new lines CR020260 are improved;(D) donor parents ' magnificent 3418B '.
Specific embodiment
Defined below and method is provided preferably to define the application and middle finger be put into practice in the application
Lead those of ordinary skill in the art.Unless otherwise mentioned, term is according to association area ordinary skill people
The common usage of member understands.
As used herein, " nucleotide sequence " includes the deoxyribose for being related to single-stranded or double-stranded form
Nucleotide or ribonucleotide polymer, and unless otherwise restriction, nucleotide sequence with 5 ' extremely
3 ' directions are write from left to right, including the known analog (example with natural nucleotide fundamental property
Such as, peptide nucleic acid(PNA)), the analog with naturally occurring nucleotide similar mode and single-stranded core
Acid hybridization.
In some embodiments, the nucleotide sequence of the application can be changed, to enter
Row conserved amino acid replacement.In certain embodiments, can be according to unifacial leaf codon preference
Property is not changed the replacement of aminoacid sequence to the nucleotide sequence of the application, for example, can use
The codon of monocotyledon preference replaces codon of the coding with amino acid sequence, and does not change
Become the aminoacid sequence coded by the nucleotide sequence.
Specifically, the application is related to SEQ ID NO:1 or SEQ ID NO:2 is further excellent
Change the nucleotide sequence of gained.The more details of the method are described in Murray etc. (1989)
Nucleic Acids Res.17:477-498.Optimization nucleotide sequence can be used to improve brown planthopper resistant base
Because of a group expression of the recombinant nucleic acid fragment in Oryza sativa L..
In some embodiments, the application further relates to SEQ ID NO:1 or SEQ ID NO:2
The variant of shown sequence.In general, the variant of specific nucleotide sequence will be with the specific nucleoside
Acid sequence is with least about 70%, 75%, 80%, 85%, 86%, 87%, 88%, 89%,
90%th, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, 99.5%
Or 99.9% or higher sequence iden, or more complementary seriess.Such variant sequence thereof
Addition, disappearance or replacement including one or more nucleic acids, it is corresponding such that it is able to cause
The addition of amino acid residue, remove or replace.By alignment programs known in the art
Sequence iden is determined including hybridization technique.The nucleotide sequence variants and the application of embodiment
The difference of sequence may be as few as 1-15 nucleotide, as little as 1-10 (such as 6-10),
As little as 5, as little as 4,3,2 or or even 1 nucleotide.
The application is further related to comprising SEQ ID NO:1 or SEQ ID NO:It is special in sequence shown in 2
The sequence of anchor point or its fragment or its variant or its complementary series, for example, comprising SEQ ID NO:
The sequence or its fragment of the 485-591 positions nucleotide of sequence shown in 1 or its variant or its complementary sequence
Row, or include SEQ ID NO:The sequence of the 629-875 positions nucleotide of sequence shown in 2 or its
Fragment or its variant or its complementary series.According to the fragment comprising above-mentioned specific site, Neng Goute
Corresponding SEQ ID NO are identified different in naturely:1 or SEQ ID NO:Sequence shown in 2.Enter one
Step ground, by identifying containing SEQ ID NO:1 or SEQ ID NO:The weight of sequence shown in 2
Group nucleic acid fragment, you can determine in testing sample comprising the recombinant nucleic acid fragment containing resistant gene.
As used herein, " Oryza sativa L. " is any rice plant including can be all with rice breeding
Plant variety.As used herein, " plant " or " plant ", including whole plant, plant cell,
Plant cell tissue cultures that plant organ, plant protoplast, plant therefrom can regenerate,
Complete plant cell in plant callus, vegetation bed and plant or plant part, the plant
Part for example embryo, pollen, ovule, seed, leaf, flower, branch, fruit, cane, root, the tip of a root,
Flower pesticide etc..
Go for any rice varieties for needing selection-breeding in the present processes.That is,
(i.e. Comprehensive Traits are preferable, it is contemplated that have and send out for the improved seeds that certain beneficial traits can be lacked by any
The kind of exhibition future) as recurrent parent.With another with beneficial traits lacking in this receptor
Kind is used as donor parents.In the embodiment of the application, using Oryza sativa L. ' Lu perfume 618B '
As recurrent parent, using the Oryza sativa L. ' magnificent 3418B ' conducts with good Brown Planthopper Resistance
Donor.
In the selection of restructuring plant provided herein, using molecular marker to restructuring
Plant carries out foreground selection.The reliability of foreground selection depends primarily on labelling and target gene group
The intersegmental chain tightness degree of piece, is the accuracy rate for improving selection, general simultaneously adjacent with both sides
Two labellings selection is tracked to target gene group fragment.
In the embodiment of the application, the foreground selection labelling of employing includes favorable selection labelling
With negative itemsets labelling, wherein, favorable selection labelling be away from target gene group fragment (containing anti-brown
Plant hopper genome) screen in the range of upstream and downstream 50kb (in Oryza sativa L. its genetic distance be 0.2cM)
Pleiomorphism molecular marker.Negative itemsets labelling is away from target gene group fragment upstream and downstream
The pleiomorphism molecular marker screened in the range of 500kb (its genetic distance is 2cM in Oryza sativa L.).
In specific embodiment, the positive foreground selection labelling of optimized Select to use is and target gene
The labelling BphC03ID03 of pack section close linkage, negative itemsets labelling is in target fragment
The molecular marker RM16165 of trip about 430kb, and dividing away from target fragment downstream about 370kb
Sub- labelling RM16211.
In the embodiment of the application, homologous recombination is carried out using above-mentioned foreground selection labelling
During detection, the criterion of side or unilateral homologous recombination is BphC03ID03 detections and ' China
The identical banding patterns of 3418B ', and RM16165 or RM16211 detections and ' Lu perfume 618B ' phases
Same banding pattern;The criterion of both sides or bilateral homologous recombination is BphC03ID03 detections and ' China
The identical banding patterns of 3418B ', and RM16175 and RM16211 detections and ' Lu perfume 618B ' phases
Same banding pattern.
In this application, it is possible to use any available chip carries out provided herein
Breeding method in Foreground selection.In preferred embodiments, the applicant can be adopted
Oryza sativa L. full-length genome breeding chip disclosed in Chinese patent application CN102747138A
RICE6K, or the Oryza sativa L. full genome disclosed in PCT international application WO/2014/121419
Group breeding chip RICE60K.Full content in this two parts of application documents is integrally incorporated to be made herein
It is reference.
Following examples are merely to illustrate and the purpose of unrestricted the application scope.If not referring in particular to
Bright, embodiment is according to conventional laboratory conditions, such as Sambrook equimoleculars Cloning: A Laboratory Manual
(Sambrook J&Russell DW,Molecular cloning:a laboratory manual,
2001), or according to the condition of manufacturer's description suggestion.
Rice plant material information used in this application can be found in rice in China kind and its
Pedigree data base (http://www.ricedata.cn/variety/index.htm).
The rice genome physical location being previously mentioned in the application is with reference to the fine genome of Oryza sativa L. Japan
MSU/TIGR annotates the 6.1st edition (http://rice.plantbiology.msu.edu/).
The open SSR molecular marker that the application is previously mentioned can be found in website
http://www.gramene.org/。
Embodiment 1Selection-breeding imports the restructuring plant of brown planthopper resistant gene pack section
Material used in the present embodiment is Oryza sativa L. ' Lu perfume 618B ' and Oryza sativa L. ' magnificent 3418B '.
' magnificent 3418B ' is with good Brown Planthopper Resistance, thus it is speculated that possibly No. 3 dye for Oryza sativa L.
Colour solid QBph3 (Hu etc., Molecular Breeding.2015,35:3) with Bph14 (Du
Deng, PNAS.2009,106 (52):Gene cluster region 22163-22168) being located is to the material
Brown Planthopper Resistance has played pivotal role.
In the Breeding Process of restructuring plant, prospect choosing is carried out to plant of recombinating using molecular marker
Select, the foreground selection molecular marker to being adopted is screened.The molecular marker portion for being used
Divide from website http://www.gramene.org/, partially self design.Method for designing is,
The 6.1st edition is annotated with reference to the fine genome MSU/TIGR of Oryza sativa L. Japan, aforementioned zones segment DNA is downloaded
Sequence.The SSR sites in above-mentioned sequence are scanned using SSRLocator softwares.Profit
With 3.0 softwares of Primer Premier to the SSR sites design primer for searching out, primer is designed altogether
128 pairs.By the method for PCR, above-mentioned primer pair is screened in ' magnificent 3418B ' and ' Lu perfume
Polymorphism in 618B ', finally picks out and has polymorphism, amplification efficiency in two parts of materials
High foreground selection molecular marker, is favorable selection labelling BphC03ID03 and negative sense choosing respectively
Select labelling RM16165, RM16211.Specifically drawing for above-mentioned molecular marker is expanded for PCR
Thing information is shown in Table 1.
1 foreground selection molecular labeling primer information of table
By ' genomic fragment that forementioned gene cluster is located in magnificent 3418B ' imports to ' Lu perfume 618B '
In, detailed process is as follows:
With ' Lu perfume 618B ' as recurrent parent, ', magnificent 3418B ' is hybridized for donor parents,
By resulting cenospecies, ' Lu perfume 618B ' is returned, and obtains BC with recurrent parent1F1
Seed, utilizes favorable selection labelling BphC03ID03 and negative itemsets labelling after nursery
RM16165, RM16211 carry out restructuring Single-plant selection, filter out 8 in target gene pack
The individual plant of section side homologous recombination, i.e. BphC03ID03 detections and ' the identical band of magnificent 3418B '
Type, and RM16165 or RM16211 detections and ' identical banding patterns of Lu perfume 618B ', and utilizing
Oryza sativa L. full-length genome breeding chip RICE6K (CN102747138A) carries out Foreground selection to which
(Yu etc., Plant Biotechnology Journal.2014,12:28-37).
The comparable chip result in the 8 unilateral homologous recombination individual plants for filtering out, selects background to return
Multiple best restructuring individual plant (this generation background recovery value is more than 75%) so as to recurrent parent ' Lu
Fragrant 618B ' is returned again, obtains BC2F1Seed, utilizes favorable selection labelling after nursery
BphC03ID03 detected to which, selects the restructuring individual plant containing target gene group fragment,
That is BphC03ID03 is detected with ' the identical banding pattern of magnificent 3418B ', is educated using Oryza sativa L. full-length genome
Planting chip RICE6K carries out Foreground selection to which.
Select background to reply preferable individual plant (this generation background recovery value is more than 87.5%) so as to
' Lu perfume 618B ' is returned again recurrent parent, obtains BC3F1Seed, profit after nursery
With favorable selection labelling BphC03ID03 and negative indicia RM16165, RM16211 to harvesting
Seed carry out the screening of target gene group fragment opposite side homologous recombination fragment, obtain 3
The individual plant of target fragment both sides restructuring, i.e. BphC03ID03 are detected with ' magnificent 3418B ' is identical
Banding pattern, and RM16165 and RM16211 detections and ' the identical banding patterns of Lu perfume 618B '.
Using Oryza sativa L. full-length genome breeding chip RICE60K (WO/2014/121419) to above-mentioned 3
Individual bilateral exchanges individual plant and carries out background and target fragment selection (Chen etc., Molecular Plant.
2014,7:541-553), screen importing target fragment less, and the target list that background is replied
One (this generation background recovery value is more than 93.75%) of strain.
By the individual plant selfing chosen once, obtain BC3F2, after nursery, utilize favorable selection labelling
BphC03ID03 detected to which, selects the individual plant containing target gene group fragment, i.e.,
BphC03ID03 is detected and ' the identical banding pattern of magnificent 3418B ', using Oryza sativa L. full-length genome breeding core
Piece RICE60K carries out Foreground selection to which.
It is final to obtain target fragment homozygosis, and background replys the strain of (background recovery value is more than 99%)
It is one, is named as CR020260.Chip detection result is shown in Fig. 1.
Embodiment 2The determination of homologous recombination fragment after importing resistance gene of brown planthopper pack section
In order to determine the brown planthopper resistant gene group clip size of importing, to ' Lu perfume 618B ' leads
The homozygosis individual plant for entering fragment has carried out the sequencing of target gene group fragment both sides homologous recombination fragment.
Brown planthopper resistant gene group recombinant nucleic acid fragment contained by CR020260 is named as
RecCR020260。
Primarily determined that by Oryza sativa L. full-length genome breeding chip RICE60K testing results,
RecCR020260 is located at two SNP markers R0335257356CA and R0335762765GA
Between.
Meanwhile, using Miseq sequencing technologies to ' Lu perfume 618B ', ' magnificent 3418B ' and
Tri- samples of CR020260 carry out genome sequencing.Using TruSeq Nano DNA LT Kit
(illumina) test kit carries out library foundation, using Library Quantification Kit-
Universal (KAPA Biosystems) test kit is carried out quantitatively, using MiSeq V2 Reagent
Kit (illumina) test kit carries out sequencing reaction.Using the desk-top sequenators of Miseq (illumina)
Detected.Concrete steps and method are referring to each test kit and sequenator operation instructions.
According to aforementioned SNP chip and Miseq sequencing results, by CR020260 brown planthopper resistant bases
Because the 35259982bp that group recombinant fragment upstream homologous recombination fragment is positioned at the 3rd chromosome is arrived
35260964bp is interval, and downstream homologous recombination fragment is positioned at 35753407bp to 35754642bp
It is interval.
On this basis, the 6.1st edition is annotated with reference to the fine genome MSU/TIGR of Oryza sativa L. Japan,
Download respective segments DNA sequence.Expanded using 5.0 software designs of Primer Premier and surveyed
Sequence primer, design requirement are long 22nt of primer or so, G/C content 40-60% and no mispairing.
With receptor parent, ' ' magnificent 3418B ' is control, right for Lu perfume 618B ' and donor parents
The upstream and downstream homologous recombination fragment of CR020260 separately designs amplimer, using high-fidelity
Enzyme KOD FX Neo (TOYOBO) is expanded, and finds optimal using two-step method or three-step approach
Amplification condition, it is ensured that amplified production is shown as single bright bar in agarose gel electrophoresiies detection
Band.The upstream homologous recombination fragment amplification primer reaction condition for wherein determining is:94℃2min;
98 DEG C of 10sec, 61 DEG C of 30sec, 68 DEG C of 60sec, 37 circulations;20℃1min.Downstream
Homologous recombination fragment amplification primer reaction condition is:94℃2min;98 DEG C of 10sec, 61 DEG C
30sec, 68 DEG C of 60sec, 37 circulations;20℃1min.Thus, two pairs are finally filtered out
Amplimer is respectively used to the amplification of upstream and downstream homologous recombination fragment.
In addition, with amplified production as template, being sequenced using Sanger sequencing, according to reality
Border is sequenced effect, and finally each filtering out 2 sequencing primers, to be respectively used to upstream and downstream homologous
The sequencing of recombinant fragment.Specific amplimer and sequencing primer sequence are shown in Table 2, sequencing result
See Fig. 2 and Fig. 3.
RecCR020260 upstreams homologous recombination sequencing fragment length is 1041bp (SEQ ID NO:
1).1-485bp is the receptor ' genomic segment of Lu perfume 618B ', with donor ' magnificent 3418B '
Relatively, there are 9 SNP, 1 Indel.This 105bp section of 486-590bp is homologous
Restructuring section.591-1041bp is donor ' magnificent 3418B ' genomic fragments, with ' Lu perfume 618B '
Relatively, there are 7 SNP, 1 Indel.
RecCR020260 downstreams homologous recombination sequencing fragment length is 1234bp (SEQ ID NO:
2).1-629bp is the donor ' genomic segment of magnificent 3418B ', with ' Lu perfume 618B ' ratios
Compared with there are 9 SNP, 2 Indel.This 245bp section of 630-874bp is homologous heavy
Group section.875-1234bp is the receptor ' genomic segment of Lu perfume 618B ', with donor ' China
3418B ' compares, and there are 4 SNP.
Structure charts of the Fig. 4 for RecCR020260 both sides homologous recombination fragment.Wherein, (A)
For upstream homologous recombination fragment structure figure;(B) it is downstream homologous recombination fragment structure figure.Top alkali
Base is that ' SNP the or InDel labellings of magnificent 3418B ', lower section base are that ' Lu is fragrant for receptor to donor
SNP the or InDel labellings of 618B '.Lycoperdon polymorphum Vitt section is from ' Lu perfume 618B ' genes
Group section, black section is from ' magnificent 3418B ' genomic segments, white section is same
Source restructuring section.Abscissa is fragment length, with base pairs (bp) as unit.
2 blast resistant gene group recombinant nucleic acid fragment amplification of table and sequencing primer information
Embodiment 3' Lu perfume 618B ' imports the Resistance Identification after brown planthopper resistant gene pack section
New lines CR020260, receptor parent in order to identify resistance effect, to the application selection-breeding
This ' Lu perfume 618B ', donor parents ' magnificent 3418B ' (as positive control), and high sense
Brown paddy plant hopper kind ' coming No. 1 in platform ' (as negative control) carries out resistance mirror in brown paddy plant hopper room
Fixed, authentication method is as follows.
Each part material is soaked seed indoors, accelerating germination, subsequently sowing pulling the plastic cover of grid line
In basin, 3 rows of every part of material point sow 45 plants altogether, and when two one heart stages of leaf, often row retains 10
Totally 30 plants of consistent plant of healthy growing way are used to connect worm for strain.Worm sources are brown come what is collected since field
Plant hopper, and captive breeding indoors.2-3 ages nymph is taken to plant to be identified, per plant has
5-10 head nymphs.When ' coming No. 1 in platform ' dead seedling 95%, start recording respectively identifies Seedling
Resistance class, take the meansigma methodss of the resistance class of 30 young plants, as the resistance class of the material,
Its resistance level is evaluated according to resistance class.Wherein, resistance class is divided into 10 grades:0 or 1 grade,
Blade is not aggrieved or first piece leaf blade tip turns to be yellow;2 grades, first piece leaf 1/2 turns to be yellow or blade tip wrinkle
Contracting;3 grades, first piece leaf turns to be yellow or withered;4 grades, second leaf portion distributes yellow or lobus cardiacus leaf
Point jaundice;5 grades, second leaf jaundice, shrinkage or withered, lobus cardiacus green grass or young crops volume;6 grades, lobus cardiacus
Curling, lobus cardiacus tip burn on leaf;7 grades, lobus cardiacus curling is withered, and plant is not dead;8 grades, lobus cardiacus
It is withered, somewhat lodge;9 grades, whole strain lodging.According to above-mentioned resistance class, 0-0.9 levels judge
For high anti-, 1.0-2.9 levels be anti-, and 3.0-5.9 levels are anti-in being, 6.0-6.9 levels are middle sense, 7.0-7.9
Level is sense, and 8.0-9.0 levels are high sense.
In brown paddy plant hopper room, Resistance Identification result is shown in Fig. 5, wherein ' coming No. 1 in platform ' is high sense,
' Lu perfume 618B ' is that sense, improvement new lines CR020260 resist in being to original kind, donor parents
' magnificent 3418B ' is high anti-.
Although above having made in detail to the application with a general description of the specific embodiments
Most description, but on the basis of the application, it can be made some modifications or improvements, this is to this
It is obvious for art personnel.Therefore, on the basis without departing from the application spirit
Upper these modifications or improvements, belong to this application claims scope.
Claims (10)
1. recombinant nucleic acid fragment, which is selected from:
I) comprising SEQ ID NO:The sequence or its fragment of the nucleotide of sequence 485-591 position shown in 1
Or its variant or its complementary series;
Ii) comprising SEQ ID NO:The sequence of sequence shown in 1 or its fragment or its variant or which is mutual
Complementary series;
Iii) comprising SEQ ID NO:The sequence or its piece of the nucleotide of sequence 629-875 position shown in 2
Section or its variant or its complementary series;
Iv) comprising SEQ ID NO:The sequence of sequence shown in 2 or its fragment or its variant or which is mutual
Complementary series;And
The combination of above fragment.
2. test right requires the primer of fragment described in 1, wherein the primer is selected from:
(I) specific recognition SEQ ID NO:The sequence of the nucleotide of sequence 1-485 position shown in 1
Forward primer and specific recognition SEQ ID NO:The nucleotide of sequence 591-1041 position shown in 1
The reverse primer of sequence;
(II) combination of first group of primer pair and second group of primer pair below, which includes
(a) first group of primer pair:Specific recognition SEQ ID NO:Sequence shown in 1
The forward primer and specific recognition SEQ ID NO of the sequence of 1-485 positions nucleotide:Sequence shown in 1
Arrange the reverse primer of the sequence of 486-590 positions nucleotide;With
(b) second group of primer pair:Specific recognition SEQ ID NO:Sequence shown in 1
The forward primer and specific recognition SEQ ID NO of the sequence of 486-590 positions nucleotide:Shown in 1
The reverse primer of the sequence of sequence 591-1041 positions nucleotide;
(III) specific recognition includes SEQ ID NO:The nucleotide of sequence 485-486 positions shown in 1
Sequence forward primer and specific recognition include SEQ ID NO:Sequence shown in 1
The reverse primer of the sequence of 590-591 positions nucleotide;
(IV) specific recognition includes SEQ ID NO:The nucleotide of sequence 485-486 positions shown in 1
Sequence forward primer and specific recognition SEQ ID NO:Sequence 591-1041 shown in 1
The reverse primer of the sequence of position nucleotide;
(V) specific recognition SEQ ID NO:The sequence of the nucleotide of sequence 1-485 positions shown in 1
Forward primer and specific recognition include SEQ ID NO:The cores of sequence 590-591 positions shown in 1
The reverse primer of the sequence of thuja acid;And/or optionally,
(VI) specific recognition SEQ ID NO:The sequence of the nucleotide of sequence 1-629 positions shown in 2
Forward primer and specific recognition SEQ ID NO:The nucleoside of sequence 875-1234 positions shown in 2
The reverse primer of the sequence of acid;
(VII) combination of the 3rd group of primer pair and the 4th group of primer pair below, which includes
(c) the 3rd group of primer pair:Specific recognition SEQ ID NO:Sequence shown in 2
The forward primer and specific recognition SEQ ID NO of the sequence of 1-629 positions nucleotide:Sequence shown in 2
Arrange the reverse primer of the sequence of 630-874 positions nucleotide;With
(d) the 4th group of primer pair:Specific recognition SEQ ID NO:Sequence shown in 2
The forward primer and specific recognition SEQ ID NO of the sequence of 630-874 positions nucleotide:Shown in 2
The reverse primer of the sequence of sequence 875-1234 positions nucleotide;
(VIII) specific recognition includes SEQ ID NO:The nucleoside of sequence 629-630 positions shown in 2
The forward primer and specific recognition of the sequence of acid includes SEQ ID NO:Sequence shown in 2
The reverse primer of the sequence of 874-875 positions nucleotide;
(IX) specific recognition includes SEQ ID NO:The nucleotide of sequence 629-630 positions shown in 2
Sequence forward primer and specific recognition SEQ ID NO:Sequence 875-1234 shown in 2
The reverse primer of the sequence of position nucleotide;
(X) specific recognition SEQ ID NO:The sequence of the nucleotide of sequence 1-629 positions shown in 2
Forward primer and specific recognition include SEQ ID NO:The cores of sequence 874-875 positions shown in 2
The reverse primer of the sequence of thuja acid.
3. test right requires the primer of fragment described in 1, wherein the primer is selected from:
(I) expand and SEQ ID NO are sequenced:The primer of sequence shown in 1
5 '-GGTCCTCTTCCTCCTCGCCTAC-3 ',
5’-TGCTTTGCCCGTTGATTGATGT-3’;And/or optionally,
(II) expand and SEQ ID NO are sequenced:The primer of sequence shown in 2
5 '-GGATTGCCTTGGTTGCTTGGTTA-3 ',
5’-TCTGTCCTTGTTTCCGTCCCTGT-3’。
4. the method that selection-breeding contains the rice plant of the recombinant nucleic acid fragment described in claim 1,
Which includes using the Oryza sativa L. recipient plant parent without genes of interest pack section as recurrent parent, incites somebody to action
Which is hybridized with the Oryza sativa L. donor plant containing genes of interest pack section, then will be resulting
Cenospecies are returned with recurrent parent, then the step of resulting backcrossing kind is carried out selfing,
Foreground selection and Foreground selection are carried out to plant of recombinating using molecular marker wherein.
5. method as claimed in claim 4, wherein for the molecular marker of the foreground selection
One or more in BphC03ID03, RM16165 and RM16211;And/or
Optionally, the Foreground selection is carried out using Oryza sativa L. full-length genome breeding chip.
6. the method as described in claim 4 or 5, wherein the recombinant nucleic acid fragment contain it is anti-
Brown paddy plant hopper gene, and the method comprising the steps of:
1) recurrent parent and donor plant are hybridized, then by resulting cenospecies and samsara
Parent is returned, and obtains first backcross generation, using favorable selection labelling BphC03ID03 and negative
The one side of brown planthopper resistant gene pack section is carried out to which to selected marker RM16165, RM16211
Homologous recombination fragment is screened, and carries out Foreground selection to which using Oryza sativa L. full-length genome breeding chip;
2) select background to reply preferably restructuring individual plant to be returned with recurrent parent again, obtain
Second backcross generation, is detected to which using favorable selection labelling BphC03ID03, select containing
The restructuring individual plant of brown planthopper resistant gene pack section, then using Oryza sativa L. full-length genome breeding chip pair
Which carries out Foreground selection;
3) select the restructuring individual plant that background is replied to be returned with recurrent parent again, obtain
Third backcross generation, using favorable selection labelling BphC03ID03 and negative itemsets labelling RM16165,
RM16211 carries out the opposite side homologous recombination fragment screening of brown planthopper resistant gene pack section to which,
And Foreground selection is carried out to which using Oryza sativa L. full-length genome breeding chip;And
4) select introgressed segment little, and the restructuring individual plant that background is replied, by the restructuring list chosen
Strain selfing once, is obtained selfed seed, which is carried out using favorable selection labelling BphC03ID03
Detection, and Foreground selection is carried out to which using Oryza sativa L. full-length genome breeding chip, finally contained
The rice plant that homozygosis brown planthopper resistant gene group recombinant nucleic acid fragment and background are replied.
7. the method as any one of claim 4 to 6, wherein using molecular marker pair
The amplimer that restructuring plant carries out adopting during foreground selection is as follows:
The primer pair of amplifier molecule labelling BphC03ID03, which includes:
Forward primer:5 '-GCAAGAATCCGACGCCATAA-3 ',
Reverse primer:5’-CTCTGCTCCTTGCTCTAATCCTCT-3’;
The primer pair of amplifier molecule labelling RM16165, which includes:
Forward primer:5 '-GGTTAACCAAGAGGAAAGGAACC-3 ',
Reverse primer:5’-GCTTTGCAACTCACTGTTGTTACG-3’;And
The primer pair of amplifier molecule labelling RM16211, which includes:
Forward primer:5 '-AATGCTAATGGCGACTGACTTCG-3 ',
Reverse primer:5’-ATGGGCTTGTTTGATTGCATCC-3’.
8. the method that test right requires the recombinant nucleic acid fragment described in 1, which includes adopting right
The primer described in 2 or 3 is required, is entered performing PCR reaction by template of testing gene group, and is analyzed
The step of PCR primer.
9. test right requires the test kit of the recombinant nucleic acid fragment described in 1, and which includes that right will
Seek the primer described in 2 or 3.
10. the rice plant containing the recombinant nucleic acid fragment described in claim 1 or seed are screened
Method, whether which is included in the genome for detect rice plant to be measured or seed containing has the right will
The step of seeking the recombinant nucleic acid fragment described in 1;
Preferably, using the primer described in Claims 2 or 3, or adopt claim 8
Described method, or using the test kit described in claim 9 being detected.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201510691321.5A CN106609276B (en) | 2015-10-22 | 2015-10-22 | Recombinant nucleic acid fragment RecCR020260 and detection method thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201510691321.5A CN106609276B (en) | 2015-10-22 | 2015-10-22 | Recombinant nucleic acid fragment RecCR020260 and detection method thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
CN106609276A true CN106609276A (en) | 2017-05-03 |
CN106609276B CN106609276B (en) | 2021-02-12 |
Family
ID=58611879
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201510691321.5A Active CN106609276B (en) | 2015-10-22 | 2015-10-22 | Recombinant nucleic acid fragment RecCR020260 and detection method thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN106609276B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109486996A (en) * | 2018-12-20 | 2019-03-19 | 华中农业大学 | Recombinant nucleotide segment Rec78801 and Rec78802 and its detection primer and application |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102586240A (en) * | 2012-02-27 | 2012-07-18 | 中国水稻研究所 | Molecular marker interlocked with rice Sogatella furcifera resisting gene and application thereof |
CN103314839A (en) * | 2013-02-27 | 2013-09-25 | 中国农业科学院烟草研究所 | Rapid target property pyramid breeding method for crops |
-
2015
- 2015-10-22 CN CN201510691321.5A patent/CN106609276B/en active Active
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102586240A (en) * | 2012-02-27 | 2012-07-18 | 中国水稻研究所 | Molecular marker interlocked with rice Sogatella furcifera resisting gene and application thereof |
CN103314839A (en) * | 2013-02-27 | 2013-09-25 | 中国农业科学院烟草研究所 | Rapid target property pyramid breeding method for crops |
Non-Patent Citations (3)
Title |
---|
KAWAHARA,Y. ET AL.: "Oryza sativa Japonica Group DNA, chromosome 3, cultivar: Nipponbare, complete sequence,GenBank: AP014959.1", 《GENBANK》 * |
张涛等: "利用产量功能基因标记分析三系杂交水稻亲本的遗传多样性", 《中国农业科学》 * |
邹声浩: "分子标记辅助改良03S的稻瘟病和褐飞虱抗性", 《中国优秀硕士学位论文全文数据库 农业科技辑》 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109486996A (en) * | 2018-12-20 | 2019-03-19 | 华中农业大学 | Recombinant nucleotide segment Rec78801 and Rec78802 and its detection primer and application |
CN109486996B (en) * | 2018-12-20 | 2019-10-01 | 华中农业大学 | Recombinant nucleotide segment Rec78801 and Rec78802 and its detection primer and application |
Also Published As
Publication number | Publication date |
---|---|
CN106609276B (en) | 2021-02-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN106480062A (en) | Recombinant nucleic acid fragment RecCR012080 and its detection method | |
CN106893769A (en) | Recombinant nucleic acid fragment RecCR012602 and its detection method | |
CN105734057A (en) | SSR mark linked with pseudoperonospora cubensis resistance main effect QTL and application of SSR mark | |
CN106609276A (en) | Recombined nucleic acid fragment RecCR020260 and detection method thereof | |
CN105567790B (en) | The selection of the plant of DNA fragmentation containing target gene group | |
CN106609273A (en) | Recombinant nucleic acid fragment RecCR020127 and detection method thereof | |
CN109486996B (en) | Recombinant nucleotide segment Rec78801 and Rec78802 and its detection primer and application | |
CN106480054A (en) | Recombinant nucleic acid fragment RecCR020322 and its detection method | |
CN106480047A (en) | Recombinant nucleic acid fragment RecCR020325 and its detection method | |
CN106480061A (en) | Recombinant nucleic acid fragment RecCR023411 and its detection method | |
CN106480057A (en) | Recombinant nucleic acid fragment RecCR012083 and its detection method | |
CN106893727A (en) | Recombinant nucleic acid fragment RecCR012600 and its detection method | |
CN107287280A (en) | Recombinant nucleic acid fragment RecCR010165 and detection method thereof | |
CN106609270A (en) | Recombinant nucleic acid fragment RecCR020264 and detection method thereof | |
CN106609272A (en) | Recombinant nucleic acid fragment RecCR020120 and detection method thereof | |
CN106609277A (en) | Recombined nucleic acid fragment RecCR020142 and detection method thereof | |
CN106480052A (en) | Recombinant nucleic acid fragment RecCR020352 and its detection method | |
CN106609278A (en) | Recombined nucleic acid fragment RecCR020141 and detection method thereof | |
CN106480055A (en) | Recombinant nucleic acid fragment RecCR020321 and its detection method | |
CN106893729A (en) | Recombinant nucleic acid fragment RecCR033207 and its detection method | |
CN107988213A (en) | Rice genome recombinant nucleic acid fragment RecCR020428 and its detection method | |
CN107988218A (en) | Rice genome recombinant nucleic acid fragment RecCR012069 and its detection method | |
CN106609271A (en) | Recombinant nucleic acid fragment RecCR02BC13 and detection method thereof | |
CN107988212A (en) | Rice genome recombinant nucleic acid fragment RecCR020429 and its detection method | |
CN106480053A (en) | Recombinant nucleic acid fragment RecCR023414 and its detection method |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant |